US10570253B2ActiveUtilityA1

Preparation method for polymer and applications thereof

42
Assignee: SOBUTE NEW MAT CO LTDPriority: Dec 31, 2015Filed: Nov 7, 2016Granted: Feb 25, 2020
Est. expiryDec 31, 2035(~9.5 yrs left)· nominal 20-yr term from priority
C08G 65/335C04B 28/02C04B 24/166C04B 2103/408C08G 65/334C08G 65/3355C04B 24/243C04B 24/246C08G 65/3322C04B 24/22C08G 65/331C08G 65/332C08G 65/3346C04B 18/08C04B 18/141C04B 2103/0088Y02W30/91
42
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Cited by
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References
16
Claims

Abstract

The present invention provides a method for preparing a polymer and a use of the polymer. The resulting polymer is used as a dispersant for an aqueous dispersion of a hydraulic binder and/or a latent hydraulic binder, such that water-reducing rate is improved, and suitable control of air content can be achieved, thereby improving the strength of concrete. The method for preparing a polymer includes polycondensation of a polyether macromonomer A of a specific structure, a monomer B and an aldehyde C to obtain the polymer. The monomer B is phenylsulfonic acid, p-/o-aminophenylsulfonic acid, p-/o-hydroxylbenzoic acid, p-/o-aminobenzoic acid, p-/o-hydroxylphenylsulfonic acid, or a phosphoric acid group or phosphorous acid group-containing monomer of a specific structure. A molar ratio of the polyether macromonomer A and the monomer B is 1:(0.5 to 12).

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
       1. A method for preparing a polymer, comprising
 performing a polycondensation of a polyether macromonomer A, a monomer B and an aldehyde C, 
 wherein the polyether macromonomer A has a structural formula (Ia), (Ib), (Ic), or (Id): 
 
       
         
           
           
               
               
           
         
         in which Z is NR 3 , O or O(CH 2 ) f O, L=O(CH 2 ) f  or (CH 2 ) f , f is an integer from 1 to 10, Q is C2 to C24 alkylene, R 2  is H or C1 to C10 alkyl, R 3  is a C1 to C10 alkyl, m=8 to 112, n=8 to 112; 
         the monomer B p-aminophenylsufonic acid, o-aminophenylsulfonic acid, p-hydroxylbenzoic acid, o-hydroxylbenzoic acid, p-aminobenzoic acid, o-aminobenzoic acid, p-hydroxylphenylsulfonic acid, o-hydroxylphenylsulfonic acid, 
         or has a structural formula (IIa) or (IIb): 
       
       
         
           
           
               
               
           
         
         in which G is N(CH 2 —PO 3 H 2 ) 2 , NH—CH 2 PO 3 H 2 , NR 6 —CH 2 PO 3 H 2 , C(OH)(PO 3 H 2 ) 2 , CH(OPO 3 H 2 )CH 2 —OPO 3 H 22 , OPO 3 H 2 , wherein 
         R 1  is H, a C1 to C10 alkyl or SO 3 H, 
         K is a C1 to C10 alkylene, 
         X=NR 8  or O, Y is OH or OR 7 , R 7  is a C1 to C10 alkyl, 
         R 6  and R 8  are independently from each other are a C1 to C10 alkyl, 
         the aldehyde C has a structural formula (III):
   R 5 CHO  (III)
 
 
         in which R 5  is H, COOH, or a C1 to C10 alkyl; and 
         a molar ratio of the polyether macromonomer A and the monomer B is 1:0.5 to 1:12, 
         wherein the polymer has a weight average molecular weight of 4000 g/mol to 150000 g/mol. 
       
     
     
       2. The method for preparing a polymer of  claim 1 , wherein,
 Z is O or O(CH 2 ) f O, f=1 to 3; 
 L is (CH 2 ) f , f=1 to 3; 
 Q is C2 to C4 alkylene; 
 R 1  is H or a C1 to C3 alkyl; 
 R 2  is H or a C1 to C3 alkyl; 
 R 3  is a C1 to C3 alkyl; 
 X is NR 8  or O; 
 R 8  is a C1 to C3 alkyl; 
 Y is OH or OR 7 ; 
 R 7  is preferably a C1 to C3 alkyl; 
 K is a C1 to C3 alkylene; and 
 R 5  is H, COOH or a C1 to C3 alkyl. 
 
     
     
       3. The method for preparing the polymer of  claim 2 , wherein the monomer B has a structural formula (IIa) or (IIb) in which G is N(CH 2 —PO 3 H 2 ) 2 , C(OH)(PO 3 H 2 ) 2 , or CH(OPO 3 H 2 )CH 2 —OPO 3 H 2 . 
     
     
       4. The method for preparing the polymer of  claim 1 , wherein the polyether macromonomer A has a molecular weight of 1000 to 10000 g/mol. 
     
     
       5. The method for preparing the polymer of  claim 1 , wherein a molar ratio of the polyether macromonomer A and the monomer B is 1:1.0 to 1:6.0. 
     
     
       6. The method for preparing the polymer of  claim 1 , wherein a molar ratio between the aldehyde C and a combinded molar amount of polyether macromonomer A and monomer B is 1.0 to 2.0. 
     
     
       7. The method for preparing the polymer of  claim 1 , wherein the conditions of the polycondensation are: a reaction temperature of 80 to 140° C. and a reaction time of 1 to 8 h. 
     
     
       8. A method of using the polymer obtained by the method of  claim 1  including
 using the polymer as a dispersant for an aqueous dispersion of a hydraulic binder and/or a latent hydraulic binder. 
 
     
     
       9. The method of  claim 8 , wherein the hydraulic binder is at least one of cement, lime, gypsum, and anhydrous gypsum, and the latent hydraulic binder is pozzolana, fly ash or blast furnace slag. 
     
     
       10. The method for preparing the polymer of  claim 1 , wherein
 the polymer has a weight average molecular weight from 8000 g/mol to 100000 g/mol. 
 
     
     
       11. The method for reparing the polymer of  claim 1 , wherein
 the polymer has a weight average molecular weight from 10000 g/mol to 40000 g/mol. 
 
     
     
       12. The method for preparing the polymer of  claim 2 , wherein
 Z is O or O(CH 2 ) f O, f=1 to 2; 
 Q is C2 to C3 alkylene; 
 R 1  is H; 
 R 2  is H; 
 R 3  is methyl; 
 R 8  is methyl or ethyl; 
 R 7  is methyl or ethyl; and 
 R 5  is H or COOH. 
 
     
     
       13. The method for preparing the polymer of  claim 3 , wherein the monomer B has a structural formula (IIa) or (IIb) in which G is N(CH 2 —PO 3 H 2 ) 2 , or C(OH)(PO 3 H 2 ) 2 . 
     
     
       14. The method for preparing the polymer of  claim 7 , wherein the conditions of the polycondensation are: the reaction temperature of 90 to 130° C. and the reaction time of 2 to 6 h. 
     
     
       15. The method of using the polymer of  claim 9 , wherein the hydraulic binder is cement. 
     
     
       16. The method for preparing the polymer of  claim 12 , wherein
 Z is O; 
 Q is CH 2 CH 2 ; 
 R 8  is methyl; 
 R 7  is methyl; and 
 R 5  is H or COOH.

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